Empregos de clinical research associate em Lisboa

TFS HealthScience is seeking a Freelance Senior Clinical Research Associate (0.15 FTE) home-based in Portugal. You will monitor sites on-site and remotely, manage ISF and CTMS, and ensure data quality while maintaining study blinding and regulatory compliance. Ideal candidates have 5+ years of on-site monitoring, ophthalmology experience, and strong...

IQVIA is seeking a Clinical Research Associate to support site selection, initiation, monitoring and close-out visits across studies. The role involves ensuring regulatory compliance and data integrity while coordinating with study sites and client representatives. The successful candidate will have a university degree in a scientific field or health care,...

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in...

Alimentiv is seeking an experienced CRA to independently perform site monitoring, coordinate visits and ensure protocol compliance in Portugal and Spain. You will mentor junior CRAs, collaborate with cross-functional teams, and participate in audits and inspections as needed. The role is home-based with regular travel (40-60%). A health sciences degree...

Clinical Research Associate Your responsibilities will include: - Performing site selection, initiation, monitoring and close-out visits - Supporting the development of a subject recruitment plan - Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.Join Our Team as a Freelance Senior Clinical Research...

Lisbon, Portugal Full time R1513619 Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and...

IQVIA in Lisbon, Portugal, is seeking a Clinical Research Associate for a full-time, on-site role. You will perform site visits, support recruitment planning, and ensure regulatory compliance while coordinating with study sites and client teams.The position requires 2-4 years of on-site monitoring experience, a university degree in a scientific field, and...

A global clinical research provider is seeking a Clinical Research Associate 2 based in Portugal. The role involves performing site selection and monitoring visits, supporting subject recruitment, and ensuring regulatory compliance. Candidates must have a relevant university degree and a minimum of two to four years' experience in monitoring. Excellent...

Clinical Research Associate 2 - Based in Portugal IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient...

IQVIA is seeking a Clinical Research Associate in Lisbon to perform site visits, support recruitment planning, and ensure regulatory compliance across study sites. You will monitor progress, manage data queries, and collaborate with site staff and client representatives to maintain trial integrity. The role requires at least 1 year of on-site monitoring...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior Clinical Research...

Lever, Inc. is seeking an experienced CRA to independently perform site monitoring activities and coordinate study execution. The role serves as the primary liaison between sponsor and investigative sites, ensuring protocol adherence and regulatory compliance. The candidate will mentor CRA I/II, participate in audits, and travel up to 60% to sites in...

Clinical Research Associate Your responsibilities will include: - Performing site selection, initiation, monitoring and close-out visits after completing training period - Supporting the development of a subject recruitment plan - Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical...

Clinical Research Associate Your responsibilities - Performing site selection, initiation, monitoring and close-out visits after completing training period - Supporting the development of a subject recruitment plan - Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and...

A leading global clinical research provider in Lisbon is seeking a Clinical Research Associate 2. This role involves performing monitoring visits, supporting subject recruitment, and ensuring regulatory compliance. Candidates should have a university degree in a scientific discipline and at least two years of monitoring experience. Strong Portuguese and...

IQVIA LLC is seeking a Clinical Research Associate to support site initiation, monitoring and close-out visits, while aiding in recruitment strategy and data integrity. Strong English/Portuguese skills and travel readiness are required. You will collaborate with study sites and client teams in a dynamic, international environment, contributing to...

- Assist in organizing, composing, and producing professional letters, summaries, reports, minutes, etc, using Microsoft Office software including Word, Access, and Excel - Proofread documents ensuring grammar, spelling, and punctuation are correct - Assist in developing capability and training presentations using PowerPoint - Create professional binders for...

What You'll Do: Assist in organizing, composing, and producing professional letters, summaries, reports, minutes, etc, using Microsoft Office software including Word, Access, and Excel Proofread documents ensuring grammar, spelling, and punctuation are correct Assist in developing capability and training presentations using PowerPoint Create...

What You'll Do: Assist in organizing, composing, and producing professional letters, summaries, reports, minutes, etc, using Microsoft Office software including Word, Access, and Excel Proofread documents ensuring grammar, spelling, and punctuation are correct Assist in developing capability and training presentations using PowerPoint Create professional...